<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Q</submitter><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><funding>Louisiana Board of Regents</funding><funding>National Institutes of Health</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>102703</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10679935</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(4)</volume><pubmed_abstract>Here, we present a protocol to isolate progenitor cells from mouse epididymal visceral adipose tissue and construct bulk RNA and assay for transposase-accessible chromatin with sequencing (ATAC-seq) libraries. We describe steps for adipose tissue collection, cell isolation, and cell staining and sorting. We then detail procedures for both ATAC-seq and RNA sequencing library construction. This protocol can also be applied to other tissues and cell types directly or with minor modifications. For complete details on the use and execution of this protocol, please refer to Liu et al. (2023).&lt;sup>1&lt;/sup>.</pubmed_abstract><journal>STAR protocols</journal><pubmed_title>Progenitor cell isolation from mouse epididymal adipose tissue and sequencing library construction.</pubmed_title><pmcid>PMC10679935</pmcid><funding_grant_id>1R01HL157519</funding_grant_id><funding_grant_id>P20GM130555</funding_grant_id><funding_grant_id>R15 DK122383</funding_grant_id><funding_grant_id>P20 GM130555</funding_grant_id><funding_grant_id>BOR.Fu.LEQSF(2019-22)-RD-A-01</funding_grant_id><funding_grant_id>1R15DK122383</funding_grant_id><funding_grant_id>R01 HL157519</funding_grant_id><pubmed_authors>Stephens JM</pubmed_authors><pubmed_authors>Shiri M</pubmed_authors><pubmed_authors>Simintiras CA</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Alkaifi F</pubmed_authors><pubmed_authors>Fu X</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Francis J</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Deng B</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Gao P</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors><pubmed_authors>Sun J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Progenitor cell isolation from mouse epididymal adipose tissue and sequencing library construction.</name><description>Here, we present a protocol to isolate progenitor cells from mouse epididymal visceral adipose tissue and construct bulk RNA and assay for transposase-accessible chromatin with sequencing (ATAC-seq) libraries. We describe steps for adipose tissue collection, cell isolation, and cell staining and sorting. We then detail procedures for both ATAC-seq and RNA sequencing library construction. This protocol can also be applied to other tissues and cell types directly or with minor modifications. For complete details on the use and execution of this protocol, please refer to Liu et al. (2023).&lt;sup>1&lt;/sup>.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-18T16:47:22.822Z</modification><creation>2025-04-07T04:12:57.567Z</creation></dates><accession>S-EPMC10679935</accession><cross_references><pubmed>37948186</pubmed><doi>10.1016/j.xpro.2023.102703</doi></cross_references></HashMap>